A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791401



Internal ID19180401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32739908..32814428hg38UCSC Ensembl
Innerchr7:32779520..32854040hg19UCSC Ensembl
Innerchr7:32746045..32820565hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3874521
hg1974521
hg1874521
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891096
Supporting Variants
Samples
Known GenesLINC00997
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791401
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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